基于UPLC-Q-TOF/MS的桂芍益宫汤体内外代谢综合分析

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Wenwen Zhou, Xiaoxiao Zhang, Meijuan Liu, Meiyu Wan, Shu Jiang, Erxin Shang, Jinao Duan
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引用次数: 0

摘要

桂芍益气汤是一种健脾益气的经典方药,几千年来一直被用于治疗脾虚。然而,其体内外代谢特性尚不清楚。本研究建立了一种基于超高效液相色谱-四极杆飞行时间质谱(UPLC-Q-TOF/MS)和自动数据处理(metabololynx)的快速可靠的分析方法,研究GYD在体内和体外的代谢产物和代谢途径。根据proton化离子的特点,检测了人参皂苷Re、人参皂苷Rg1、人参皂苷Rb1、白术内酯I、白术内酯III、芍药苷、甘草酸、厚皮酸、甘草素、白皮素、阿魏酸等11种前体及其代谢产物,并初步鉴定。共鉴定出81种代谢物,其中53种为体内代谢物,40种为肝微粒体代谢物,43种为体外肠道菌群代谢物。在肠道菌群和肝微粒体之间观察到不同的代谢模式——前者主要催化I期转化(羟基化、甲基化、去羟基化、去甲基化和还原),而后者也进行II期代谢,葡萄糖醛酸化是主要的偶联反应。系统分析GYD有效成分的代谢谱和代谢途径,有助于阐明其潜在机制和临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive analysis of the in vivo and in vitro metabolism of Guishao Yigong Decoction based on UPLC-Q-TOF/MS
Guishao Yigong Decoction (GYD), a classic prescription that tonifies the spleen and qi, has been used in clinical practices for thousands of years to treat spleen deficiency. However, its in vitro and in vivo metabolic characteristics are still unclear. In this study, a rapid and reliable analytical method based on ultra-high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS) with automated data processing (MetaboLynx) was established to investigate the metabolites and metabolic pathways of GYD in vivo and in vitro. Based on the characteristics of protonated ions, eleven precursors (ginsenoside Re, ginsenoside Rg1, ginsenoside Rb1, atractylenolide I, atractylenolide III, paeoniflorin, glycyrrhizic acid, pachymic acid, liquiritin, nobiletin, and ferulic acid) and their corresponding metabolites were detected and tentatively identified. A total of 81 metabolites were identified, including 53 metabolites in vivo, 40 metabolites of liver microsomes, and 43 metabolites of intestinal flora in vitro. Distinct metabolic patterns were observed between intestinal flora and liver microsomes - the former primarily catalyzed phase I transformations (hydroxylation, methylation, dehydroxylation, demethylation, and reduction), while the latter also executed phase II metabolism, with glucuronidation being the predominant conjugation reaction. The metabolic profiling and pathways of active components in GYD were systematically analyzed, which was helpful in clarifying its potential mechanism and clinical application.
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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